FDA Adverse Event Malfunction Summary report: N

COMPOUNDERS

MDR report key: 2738468 · Received September 10, 2012

Report

Report Number
6000001-2012-14005
Event Type
Malfunction
Date Received
September 10, 2012
Date of Event
August 17, 2012
Report Date
August 17, 2012
Manufacturer
BAXTER HEALTHCARE - LARGO
Product Code
NEP
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). EVALUATION SUMMARY:THE REPORTED CONDITION OF "THE FLUSH KEY ON THE KEYPAD IS NOT WORKING" WAS CONFIRMED AND REPRODUCED DURING DEVICE EVALUATION. THE ROOT CAUSE WAS DUE TO A MISSING NYLON WASHER ELECTRODE. THE NYLON WASHER ELECTRODE WAS INSTALLED TO CORRECT THE REPORTED CONDITION.

Additional Manufacturer Narrative · 1

(B)(4). INITIAL EVALUATION CONFIRMED THE REPORTED CONDITION. UPON COMPLETION OF BAXTER'S INVESTIGATION, A FOLLOW-UP WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE WAS RETURNED TO BAXTER AND IS CURRENTLY IN THE PROCESS OF BEING EVALUATED. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF THE EVALUATION OR IF ANY ADDITIONAL DETAILS BECOME AVAILABLE. THIS DEVICE IS CLASS II EXEMPT FROM HAVING A 510(K) NUMBER. ITS ADDITIONAL 510(K) NUMBER IS K961008.

Description of Event or Problem · 1

BAXTER RECEIVED A REPORT FROM A FACILITY INVOLVING AN AUTOMIX 3+3/AS COMPOUNDER. ACCORDING TO THE FACILITY, THE FLUSH KEY ON THE KEYPAD IS NOT WORKING. THIS EVENT OCCURRED DURING SETUP IN THE PHARMACY. THE UNIT IS BEING SWAPPED. THERE WAS NO PATIENT INVOLVEMENT; THEREFORE, NO PATIENT INJURY, MEDICAL INTERVENTION, OR ADVERSE REACTION IS ASSOCIATED WITH THE REPORTED CONDITION. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COMPOUNDERS SYSTEM/DEVICE, PHARMACY COMPOUNDING NEP BAXTER HEALTHCARE - LARGO

Patients

Seq Age Sex Outcome Treatment
1